Darnerud P O
Acta Pharmacol Toxicol (Copenh). 1984 Aug;55(2):110-5. doi: 10.1111/j.1600-0773.1984.tb01971.x.
The degradation of 1-14C-chlorododecanes to 14CO2 in C57BL mice was studied. 1-14C-Chlorododecane-injected mice were transferred to an all-glass metabolism cage and the exhaled air was monitored for 14CO2. Pretreatment with cytochrome P-450 inhibitors resulted in a marked decrease in the rate of 14CO2-formation, when measured as peak 14CO2-exhalation rate (PER): After piperonyl butoxide pretreatment the degradation rate of a high-chlorinated 14C-dodecane (PCDD II; 68% Cl w/w) to 14CO2 was 16% of control, and after metyrapone pretreatment 40%. It was also shown that piperonyl butoxide pretreatment decreased the rate of 14CO2-formation, and the amount of 14CO2 formed, in proportion to the chlorine content of four differently chlorinated dodecanes. The cytochrome P-450 inducer phenobarbital moderately (PER 152%) increased the rate of 14CO2-formation from PCDD II, whereas 3-methylcholanthrene and several technical grade chlorinated paraffins generally gave less or no inductive effects. Also the cumulative 14CO2-exhalation, measured during six hours (CE-6), was inhibited and induced after the above pretreatments. The results indicate a cytochrome P-450-dependent degradation of C12-chloroalkanes to 14CO2 in vivo. The degradation via cytochrome P-450 seems to be relatively more important for higher chlorinated alkanes.
研究了C57BL小鼠体内1-¹⁴C-氯代十二烷降解为¹⁴CO₂的情况。给注射了1-¹⁴C-氯代十二烷的小鼠转移到全玻璃代谢笼中,监测呼出气体中的¹⁴CO₂。用细胞色素P-450抑制剂预处理后,以¹⁴CO₂呼出峰值速率(PER)衡量,¹⁴CO₂形成速率显著降低:在用胡椒基丁醚预处理后,高氯代¹⁴C-十二烷(PCDD II;68% Cl w/w)降解为¹⁴CO₂的速率为对照的16%,在用甲吡酮预处理后为40%。还表明,胡椒基丁醚预处理降低了¹⁴CO₂的形成速率以及形成的¹⁴CO₂量,且与四种不同氯代十二烷的氯含量成比例。细胞色素P-450诱导剂苯巴比妥适度(PER为152%)提高了PCDD II产生¹⁴CO₂的速率,而3-甲基胆蒽和几种工业级氯化石蜡通常产生的诱导作用较小或无诱导作用。上述预处理后,六小时内测得的累积¹⁴CO₂呼出量(CE-6)也受到抑制或诱导。结果表明,体内C₁₂-氯代烷烃降解为¹⁴CO₂依赖于细胞色素P-450。对于高氯代烷烃,通过细胞色素P-450的降解似乎相对更重要。